I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
Stock No. | Größe | Preis ($) | Menge | Verfügbarkeit |
---|---|---|---|---|
A15568-14 | 25g | 40,10 |
|
|
A15568-22 | 100g | 117,00 |
|
|
A15568-36 | 500g | 507,00 |
|
|
It is mainly used in biochemical reaction and used as medicine intermediate. It is used in synthesize for below products: L-gulose;1,2:5,6-Di-O-isopropylidene-a-D-gulofuranose; Alllose; ;1,2:5,6-Double-O-Isopropylidene-3-C-(1-Methoxycarbonyl)Ethide-alfa-D-Furanose) ;1,2:5,6-Di-O-isopropylidene-a-D-ribo-hexofuranose-3-ulose;6-deoxy idose.
I. Fernandez, et al. Asymmetric synthesis of alkane- and arenesulfinates of diacetone-D-glucose (DAG): an improved and general route to both enantiomerically pure sulfoxides.J. Org. Chem.,1992,57(25), 6789-6796.
Tadashi Eguchi, et al. The overman rearrangement on a diacetone-D-glucose template: kinetic and theoretical studies on the chirality transcription.Tetrahedron.,1993,49(21), 4527-4540.
Chiral auxiliary in a general route to enantiomerically pure sulfoxides: J. Org. Chem., 57, 6789 (1992). For an improved method for methyl p-tolyl sulfoxide, see: Synthesis, 761 (1995).
Gefahrenhinweise (EU): H303
May be harmful if swallowed.
Sicherheitshinweise: P312a
Call a POISON CENTER/doctor if you feel unwell.